Disproven
Methylphenidate: improve symptoms or function in MS (type not specified)
MS (type not specified) · Fatigue / wakefulness
Placebo-controlled phase 3 trials missed their main goal, and none succeeded. This applies to this patient group only.
- Trials
- 3
- Running now
- 0
- Controlled phase 2/3 trials
- 3
- People in controlled trials
- 261
Deciding trials (phase 3): 0 met, 1 did not.
Other linked trials: 2
Dose comparisons, trials against another medicine, add-on trials, phase 1 and uncontrolled studies. They are listed below but do not set the status.
Trials
Phase 3 · 2017 · Placebo-controlled · MSFT-NCT03185065
The estimated mean values of MFIS total scores at baseline and the maximal tolerated dose were as follows: 51·3 (95% CI 49·0-53·6) at baseline, 40·6 (38·2-43·1) with placebo, 41·3 (38·8-43·7) with amantadine, 39·0 (36·6-41·4) with modafinil, and 38·6 (36·2-41·0) with methylphenidate (p=0·20 for the overall medication effect in the linear mixed-effect regression model).
Read by software from the paper's abstractPhase 2/3 · 2013 · Placebo-controlled · MSFT-NCT01896700
Other linked trials: 2
These linked trials do not set the status.
- MSNo result found
Phase 2 · 2012 · Placebo-controlled
The deciding phase and counts come from the Trial Bank’s fixed rules.
Lab evidence
Lab studies in animals or cells. Results in animals often do not hold in people, and these studies never change the status of an idea.
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History
- 2026-10-28Status changed from Results pending to Disproven
- 2026-10-27First listed as Results pending
Related hypotheses
- Amantadine: improve symptoms or function in MS (type not specified)
- Methylphenidate: improve symptoms or function in relapsing MS
- Methylphenidate: improve symptoms or function in relapsing and progressive MS
- Modafinil: improve symptoms or function in MS (type not specified)
- Solriamfetol: improve symptoms or function in MS (type not specified)
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